Isochromosome - CISMeF

Preferred Label : Isochromosome;

NCIt definition : An abnormal chromosome with identical arms, formed by transverse splitting of the centromere during chromosomal replication.;

Details

Origin ID

C3897;

UMLS CUI

C0242621;

Automatic exact mappings (from CISMeF team)
- Isocromosoma [PASCAL descriptor]
Currated CISMeF NLP mapping
- isochromosomes [MeSH Descriptor]
- isochromosomes [MeSH concept]
Semantic type(s)
- Acquired Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- isochromosomes [MeSH concept]
- isochromosomes [MeSH Descriptor]

Keyword's position in hierarchy(ies) :

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